Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 1.0647 | 1 | 1 |
Echinococcus multilocularis | insulin receptor | 0.0153 | 0.0078 | 0.0078 |
Schistosoma mansoni | tyrosine kinase | 0.0153 | 0.0078 | 0.0078 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 1.0647 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.024 | 0.0161 | 0.0161 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.0012 | 0.0012 |
Brugia malayi | Protein kinase domain containing protein | 0.0085 | 0.0014 | 0.0014 |
Loa Loa (eye worm) | TK/ALK protein kinase | 0.0275 | 0.0194 | 0.0194 |
Brugia malayi | Protein kinase domain containing protein | 0.0153 | 0.0078 | 0.0078 |
Schistosoma mansoni | sodium-bile acid cotransporter | 0.633 | 0.5918 | 0.5918 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.0153 | 0.0078 | 0.0078 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.4317 | 0.4015 | 0.4015 |
Loa Loa (eye worm) | TK/INSR protein kinase | 0.0153 | 0.0078 | 0.0078 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Onchocerca volvulus | 1.0647 | 1 | 0.5 | |
Brugia malayi | Protein kinase domain containing protein | 0.0276 | 0.0194 | 0.0194 |
Echinococcus granulosus | insulin growth factor 1 receptor beta | 0.0153 | 0.0078 | 0.0078 |
Echinococcus multilocularis | insulin growth factor 1 receptor beta | 0.0153 | 0.0078 | 0.0078 |
Echinococcus granulosus | insulin receptor | 0.0153 | 0.0078 | 0.0078 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.0647 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Duration (functional) | = 8.6 min | Duration of analgesic effect using mouse hot plate assay | ChEMBL. | 2170652 |
Duration (functional) | = 8.6 min | Duration of analgesic effect using mouse hot plate assay | ChEMBL. | 2170652 |
ED50 (functional) | = 0.1125 mg kg-1 | Analgesic activity using mouse hot plate technique at 55 degree centigrade | ChEMBL. | 2170652 |
ED50 (functional) | = 0.1125 mg kg-1 | Analgesic activity using mouse hot plate technique at 55 degree centigrade | ChEMBL. | 2170652 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.